P
US9029083B2ExpiredUtilityPatentIndex 98

Vitro evolution in microfluidic systems

Assignee: GRIFFITHS ANDREW DAVIDPriority: Oct 8, 2004Filed: Oct 10, 2005Granted: May 12, 2015
Est. expiryOct 8, 2024(expired)· nominal 20-yr term from priority
Inventors:GRIFFITHS ANDREW DAVIDWEITZ DAVIDLINK DARRENAHN KEUNHOBIBETTE JEROME
B01L 2300/0816B01J 2219/00468B01J 2219/005B01J 2219/00545B01J 2219/00576C12Q 1/6874B01L 2200/0673G01N 15/1459C12N 15/1058B01L 3/502753B01L 2400/0487B01L 2300/0864C12P 21/00B01J 2219/00466B01L 2400/0415B01J 2219/00722B01J 2219/00657G01N 15/1484B01L 3/502776B01J 2219/0052B01L 3/502746B01L 2300/0654B01J 19/0046B01L 3/502784B01L 2300/0867C12N 15/1075B01L 2200/0636B01F 3/0807B01F 13/0071B01F 5/0647B01F 13/0076B01F 5/0655B01F 13/0062B01F 5/0646B01F 23/41B01F 25/4338B01F 25/4331B01F 33/3011B01F 33/3021B01F 33/3031B01F 25/433G01N 15/149
98
PatentIndex Score
269
Cited by
1,574
References
11
Claims

Abstract

The invention describes a method for isolating one or more genetic elements encoding a gene product having a desired activity, comprising the steps of: (a) compartmentalising genetic elements into microcapsules; and (b) sorting the genetic elements which express the gene product having the desired activity; wherein at least one step is under microfluidic control. The invention enables the in vitro evolution of nucleic acids and proteins by repeated mutagenesis and iterative applications of the method of the invention.

Claims

exact text as granted — not AI-modified
The invention claimed is: 
     
       1. A method for providing a library of entities, comprising the steps of:
 producing a plurality of aqueous droplets by partitioning an aqueous fluid as it is flowing through a channel with an immiscible continuous phase that comprises a fluorinated oil and a fluorinated polymer surfactant, each droplet comprising at least one entity; and 
 pooling the droplets into one or more common compartments that have larger cross-sectional areas than the channel that slows the velocity of the droplets as compared to their velocity within the channel, wherein the droplets contact each other but do not fuse within the one or more common compartments, thereby providing a library of encapsulated entities. 
 
     
     
       2. The method of  claim 1 , wherein the entities are nucleic acids, proteins, or cells. 
     
     
       3. The method of  claim 2 , wherein the nucleic acids are primers for a polymerase chain reaction (PCR). 
     
     
       4. The method of  claim 1 , wherein the entities are labeled. 
     
     
       5. The method of  claim 4 , wherein the entities are optically labeled. 
     
     
       6. The method of  claim 1 , wherein the entities are fluorescently labeled antibodies. 
     
     
       7. The method of  claim 1 , wherein the entities are chemically labeled antibodies. 
     
     
       8. The method of  claim 1 , wherein the droplets are unable to fuse due to the presence of a surfactant. 
     
     
       9. The method of  claim 1 , wherein the droplets are separated by the immiscible continuous phase in the channel. 
     
     
       10. The method of  claim 1 , wherein the oil is a perfluorinated oil. 
     
     
       11. The method of  claim 1 , wherein the droplets are monodisperse with respect to each other.

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